Canonical Allele Identifier: CA380702479
Community Standard Title: NM_015457.3(ZDHHC5):c.605G>A (p.Gly202Asp)
Gene: ZDHHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57690382G>A , CM000673.2:g.57690382G>A GRCh38
NC_000011.9:g.57457854G>A , CM000673.1:g.57457854G>A GRCh37
NC_000011.8:g.57214430G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015457.3:c.605G>A MANE Select NP_056272.2:p.Gly202Asp
ENST00000287169.8:c.605G>A MANE Select ENSP00000287169.3:p.Gly202Asp
NM_015457.2:c.605G>A NP_056272.2:p.Gly202Asp
ENST00000287169.7:c.605G>A ENSP00000287169.3:p.Gly202Asp
ENST00000527985.5:c.446G>A ENSP00000432202.1:p.Gly149Asp
ENST00000528177.5:c.299G>A ENSP00000431209.1:p.Gly100Asp
ENST00000529447.1:c.162+1717G>A ENSP00000435722.1:n.162+1717G>A
ENST00000529480.1:n.852G>A
ENST00000532842.1:c.299G>A ENSP00000435593.1:p.Gly100Asp
XM_011544899.1:c.605G>A XP_011543201.1:p.Gly202Asp
XM_011544900.1:c.605G>A XP_011543202.1:p.Gly202Asp
XM_011544901.1:c.605G>A XP_011543203.1:p.Gly202Asp
XM_017017498.2:c.299G>A XP_016872987.1:p.Gly100Asp
XR_001747825.2:n.1753G>A